Circulating Inhibitor against Factor X: A Rare Cause of Hemorrhagic Diathesis.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI:10.1155/2023/5510654
P Rossignon, F Grandjean, A Claessens, N Weynants
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引用次数: 0

Abstract

Acquired coagulopathies resulting from factor X deficiency are rare and typically associated with amyloidosis or plasma cell dyscrasia. Factor X plays a pivotal role in the coagulation cascade, converting prothrombin into thrombin and facilitating the formation of fibrinogen and thrombus. While its occurrence following common infections is extremely rare, isolated cases have been documented. We present a rare case of bleeding diathesis in a patient with community-acquired pneumonia, where prolonged activated partial thromboplastin time (aPTT) and prothrombin time (PT) led to the diagnosis of an infectious-triggered acquired circulating inhibitor targeting factor X. Prompt treatment with methylprednisolone effectively controlled the inhibitor without recurrence. This case report provides insights into the diagnostic strategies, differential algorithm, and therapeutic approaches for managing this rare coagulopathy.

针对因子 X 的循环抑制剂:出血综合症的罕见病因
因因子 X 缺乏而导致的获得性凝血病很少见,通常与淀粉样变性或浆细胞发育不良有关。因子 X 在凝血级联过程中起着关键作用,可将凝血酶原转化为凝血酶,促进纤维蛋白原和血栓的形成。虽然在普通感染后出现这种情况极为罕见,但也有个别病例记录在案。我们报告了一例罕见的社区获得性肺炎患者出血综合征病例,患者活化部分凝血活酶时间(aPTT)和凝血酶原时间(PT)延长,诊断为感染引发的获得性循环抑制因子 X。本病例报告深入介绍了治疗这种罕见凝血病的诊断策略、鉴别算法和治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
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51
审稿时长
13 weeks
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